K023173 is an FDA 510(k) clearance for the ANDREWS INTRODUCER, MODEL ASI01. This device is classified as a Instrument, Manual, Surgical, General Use (Class I - General Controls, product code MDM).
Submitted by Andrews Surgical Innovations, Ltd. (Co. Dublin, IE). The FDA issued a Cleared decision on December 18, 2002, 86 days after receiving the submission on September 23, 2002.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4800.
| 510(k) Number | K023173 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 23, 2002 |
| Decision Date | December 18, 2002 |
| Days to Decision | 86 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | MDM — Instrument, Manual, Surgical, General Use |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 878.4800 |